Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000605563 | SCV000712308 | likely benign | not specified | 2016-08-04 | criteria provided, single submitter | clinical testing | c.2506+15C>G in intron 17 of MYOM1: This variant is not expected to have clinica l significance because it is not located within the splice consensus sequence. |